Validation of a measure of family experience of patients with serious illness: the QUAL-E (Fam).
dc.contributor.author | Steinhauser, Karen E | |
dc.contributor.author | Voils, Corrine I | |
dc.contributor.author | Bosworth, Hayden B | |
dc.contributor.author | Tulsky, James A | |
dc.date.accessioned | 2024-02-01T15:21:38Z | |
dc.date.available | 2024-02-01T15:21:38Z | |
dc.date.issued | 2014-12 | |
dc.description.abstract | ContextFamily members of seriously ill patients experience significant burden as they advocate with providers and participate in key decisions for loved ones. Most assessments focus on patient experience, yet family members' own quality of experience is central to comprehensive care.ObjectivesThis study validated a measure of the quality of family experience, the QUAL-E (Fam), in palliative care.MethodsWe enrolled family members of terminally ill patients admitted to general medicine services at two hospitals. Items were based on foundational work originally done for the patient instrument, QUAL-E, and interviews of family members of terminally ill patients. Cognitive interviewing was used to refine items, which then underwent formal testing factor analysis. In the first sample, we assessed factor structure. A subsequent sample established predictive validity and test-retest reliability.ResultsThe initial item pool was reduced to a four-domain, 35-item scale and administered to the validation sample. Further analyses produced a final brief scale comprising 17 items, demonstrating appropriate convergent and divergent validity. Test-retest reliability demonstrated expected levels of stability in a highly changeable population. The scale provides an assessment of family experience and includes subscales assessing relationship with health care provider and completion. Additional scale items assess symptom experience and issues of preparation.ConclusionThe QUAL-E (Fam) is a companion instrument to the patient QUAL-E measure of quality of life at the end of life and is part of a package of assessment tools that can help evaluate the entire patient experience and contribute to quality care. | |
dc.identifier | S0885-3924(14)00254-1 | |
dc.identifier.issn | 0885-3924 | |
dc.identifier.issn | 1873-6513 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | Journal of pain and symptom management | |
dc.relation.isversionof | 10.1016/j.jpainsymman.2014.04.006 | |
dc.rights.uri | ||
dc.subject | Humans | |
dc.subject | Palliative Care | |
dc.subject | Factor Analysis, Statistical | |
dc.subject | Reproducibility of Results | |
dc.subject | Family | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Interviews as Topic | |
dc.subject | Surveys and Questionnaires | |
dc.title | Validation of a measure of family experience of patients with serious illness: the QUAL-E (Fam). | |
dc.type | Journal article | |
duke.contributor.orcid | Bosworth, Hayden B|0000-0001-6188-9825 | |
pubs.begin-page | 1168 | |
pubs.end-page | 1181 | |
pubs.issue | 6 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Faculty | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Psychiatry & Behavioral Sciences | |
pubs.organisational-group | Medicine, General Internal Medicine | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Center for the Study of Aging and Human Development | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Duke Science & Society | |
pubs.organisational-group | Population Health Sciences | |
pubs.organisational-group | Duke Innovation & Entrepreneurship | |
pubs.organisational-group | Psychiatry & Behavioral Sciences, Behavioral Medicine & Neurosciences | |
pubs.organisational-group | Duke - Margolis Center For Health Policy | |
pubs.publication-status | Published | |
pubs.volume | 48 |